Canonical Allele Identifier: CA2154909544

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279433_91279434delinsGA , CM000676.2:g.91279433_91279434delinsGA	GRCh38
NC_000014.8:g.91745777_91745778delinsGA , CM000676.1:g.91745777_91745778delinsGA	GRCh37
NC_000014.7:g.90815530_90815531delinsGA	NCBI36
NG_033118.1:g.143411_143412delinsTC
NG_033118.2:g.143411_143412delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-128_4700-127delinsTC MANE Select	ENSP00000374507.6:n.4700-128_4700-127delinsTC
ENST00000331194.8:c.272-128_272-127delinsTC	ENSP00000330332.8:n.272-128_272-127delinsTC
ENST00000334448.5:n.512-128_512-127delinsTC
ENST00000389857.10:c.4700-128_4700-127delinsTC	ENSP00000374507.6:n.4700-128_4700-127delinsTC
ENST00000556726.5:c.928-128_928-127delinsTC
ENST00000557455.1:n.544_545delinsTC
NM_001080414.3:c.4700-128_4700-127delinsTC	NP_001073883.2:n.4700-128_4700-127delinsTC
XM_011536796.1:c.4592-128_4592-127delinsTC	XP_011535098.1:n.4592-128_4592-127delinsTC
XR_429316.2:n.4975-128_4975-127delinsTC
XR_943459.1:n.5455_5456delinsTC
XM_011536796.2:c.4592-128_4592-127delinsTC	XP_011535098.1:n.4592-128_4592-127delinsTC
XM_017021335.2:c.*446_*447delinsTC	XP_016876824.1:n.*446_*447delinsTC
XM_017021336.1:c.1781-128_1781-127delinsTC	XP_016876825.1:n.1781-128_1781-127delinsTC
XR_429316.4:n.4973-128_4973-127delinsTC
NM_001080414.4:c.4700-128_4700-127delinsTC MANE Select	NP_001073883.2:n.4700-128_4700-127delinsTC